Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
DLK1	gene	DLK1	Expert Review Amber;Literature	Genomic imprinting			MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)					30794780;18271756;http://igc.otago.ac.nz/home.html;29641995		False	2	50;50;0	0.157	False		ENSG00000185559	ENSG00000185559	HGNC:2907													
PEG3	gene	PEG3	Expert Review Amber;Literature	Genomic imprinting			MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	dysmorphic features;developmental delay				30007940;32169557;31639176;29734399;30794780;http://igc.otago.ac.nz/home.html		False	2	0;100;0	0.157	False		ENSG00000198300	ENSG00000198300	HGNC:8826